Department of Pharmaceutical Sciences, College of Pharmacy, 203 Pharmacy Building, Oregon State University, Corvallis, Oregon 97331, USA.
J Org Chem. 2012 Jul 20;77(14):6066-75. doi: 10.1021/jo3008622. Epub 2012 Jul 3.
Mandelalides A-D are variously glycosylated, unusual polyketide macrolides isolated from a new species of Lissoclinum ascidian collected from South Africa, Algoa Bay near Port Elizabeth and the surrounding Nelson Mandela Metropole. Their planar structures were elucidated on submilligram samples by comprehensive analysis of 1D and 2D NMR data, supported by mass spectrometry. The assignment of relative configuration was accomplished by consideration of homonuclear and heteronuclear coupling constants in tandem with ROESY data. The absolute configuration was assigned for mandelalide A after chiral GC-MS analysis of the hydrolyzed monosaccharide (2-O-methyl-α-L-rhamnose) and consideration of ROESY correlations between the monosaccharide and aglycone in the intact natural product. The resultant absolute configuration of the mandelalide A macrolide was extrapolated to propose the absolute configurations of mandelalides B-D. Remarkably, mandelalide B contained the C-4' epimeric 2-O-methyl-6-dehydro-α-L-talose. Mandelalides A and B showed potent cytotoxicity to human NCI-H460 lung cancer cells (IC(50), 12 and 44 nM, respectively) and mouse Neuro-2A neuroblastoma cells (IC(50), 29 and 84 nM, respectively).
曼德拉利德斯 A-D 是从南非阿尔戈阿湾伊丽莎白港附近和周围的纳尔逊·曼德拉大都市新收集的裂殖壶菌属中分离出来的各种糖基化的、不寻常的聚酮大环内酯。通过对亚毫克级样品的全面分析,包括一维和二维 NMR 数据以及质谱,阐明了它们的平面结构。相对构型的分配是通过考虑同核和异核耦合常数以及 ROESY 数据来完成的。在对水解的单糖(2-O-甲基-α-L-鼠李糖)进行手性 GC-MS 分析并考虑完整天然产物中单糖和糖苷之间的 ROESY 相关之后,确定了曼德拉利德斯 A 的绝对构型。曼德拉利德斯 A 大环内酯的结果绝对构型被推断为曼德拉利德斯 B-D 的绝对构型。值得注意的是,曼德拉利德斯 B 含有 C-4' 差向异构的 2-O-甲基-6-去氢-α-L-塔洛糖。曼德拉利德斯 A 和 B 对人 NCI-H460 肺癌细胞(IC(50)分别为 12 和 44 nM)和小鼠神经母细胞瘤 Neuro-2A 细胞(IC(50)分别为 29 和 84 nM)表现出很强的细胞毒性。